Variant #0001005597 (NC_000020.10:g.62326867A>G, NC_000020.10(NM_016434.3):c.3652+34A>G (RTEL1))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.62326867A>G
DNA change (hg38) -
Published as RTEL1(NM_001283009.1):c.3686A>G (p.(Gln1229Arg))
ISCN -
DB-ID ARFRP1_000138
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZGPAT NM_001083113.1 -?/. - c.-12073A>G r.(?) p.(=)
ARFRP1 NM_001134758.2 -?/. - c.*5083T>C r.(=) p.(=)
TNFRSF6B NM_003823.3 -?/. - c.-1254A>G r.(?) p.(=)
RTEL1 NM_016434.3 -?/. - c.3652+34A>G r.(=) p.(=)
RTEL1-TNFRSF6B NR_037882.1 -?/. - n.4513A>G r.(?) -


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